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Published in Movement disorders (01.04.2012)
Published in Movement disorders (01.04.2012)
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Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literature
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Published in Neurocase (01.02.2013)
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Detection of EGFR Mutations in Circulating Tumor DNA (ctDNA) Retrieved from Plasma - Interlaboratory Quality Assessment in the Czech Republic
Linda, Čapková, Markéta, Kalinová, Ivana, Tichá, Eva, Parobková, Milada, Matějčková, Hana, Vošmiková, Ondřej, Horký, Karolína, Bartáková, Jiří, Drábek, Monika, Bajerová, Pavel, Dundr
Published in Klinická onkologie (2018)
Published in Klinická onkologie (2018)
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Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's disease
Fiala, Ondrej, Zahorakova, Daniela, Pospisilova, Lenka, Kucerova, Jana, Matejckova, Milada, Martasek, Pavel, Roth, Jan, Ruzicka, Evzen
Published in PloS one (19.09.2014)
Published in PloS one (19.09.2014)
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Molecular pathology of pulmonary carcinomas
Rohan, Zdeněk, Matějčková, Milada, Matěj, Radoslav
Published in Ceskoslovenské patologie (01.04.2014)
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Published in Ceskoslovenské patologie (01.04.2014)
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Malignant Melanoma - from Classical Histology towards Molecular Genetic Testing
Ryška, A, Horký, O, Berkovcová, J, Tichá, I, Kalinová, M, Matějčková, M, Bóday, Á, Drábek, J, Martínek, P, Šimová, J, Sieglová, K, Vošmiková, H
Published in Klinická onkologie (2017)
Published in Klinická onkologie (2017)
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Parkin
Fiala, Ondrej, Zahorakova, Daniela, Pospisilova, Lenka, Kucerova, Jana, Matejckova, Milada, Martasek, Pavel, Roth, Jan, Ruzicka, Evzen
Published in PloS one (19.09.2014)
Published in PloS one (19.09.2014)
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Gerstmann-Straeussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literature
Rusina, Robert, Fiala, Jindrich, Holada, Karel, Matejckova, Milada, Novakova, Jana, Ampapa, Radek, Koukolik, Frantisek, Matej, Radoslav
Published in Neurocase (01.01.2013)
Published in Neurocase (01.01.2013)
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Parkin mutations and phenotypic features in Czech patients with early-onset Parkinson's disease
Fiala, Ondrej, Pospisilova, Lenka, Prochazkova, Jana, Matejckova, Milada, Martasek, Pavel, Novakova, Lucie, Roth, Jan, Ruzicka, Evzen
Published in Neuro-endocrinology letters (2010)
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Published in Neuro-endocrinology letters (2010)
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QF-PCR Examination of Parental and Meiotic Origin of Trisomy 21 in Central and Eastern Europe
Machatkova, Marina, Brouckova, Martina, Matejckova, Milada, Krebsova, Alice, Sperling, Karl, Vorsanova, Svetlana, Kutsev, Sergei, Zerova, Tatiana, Arbuzova, Svetlana, Krejci, Roman, Petersen, Michael, Macek, Milan, Sr
Published in The journal of histochemistry and cytochemistry (01.03.2005)
Published in The journal of histochemistry and cytochemistry (01.03.2005)
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KRAS mutation testing in therapeutic algorithm for treatment of metastatic colorectal carcinoma
Dubská, Lenka, Vyskocilová, Martina, Nenutil, Rudolf, Valík, Dalibor, Knoflícková, Dana, Fabian, Pavel, Kocáková, Ilona, Demlová, Regina, Beránek, Martin, Drastíková, Monika, Vosmiková, Hana, Bóday, Arpád, Horká, Katerina, Símová, Jarmila, Drábek, Jirí, Ehrmann, Jirí, Hajdúch, Marián, Matejcková, Milada, Síma, Radek, Tvrdík, Daniel, Povýsil, Ctibor, Ryska, Ales
Published in Časopis lékařů českých (2011)
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Published in Časopis lékařů českých (2011)
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